A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111870



Internal ID18903789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:77041144..77041463hg38UCSC Ensembl
Outerchr10:78800902..78801221hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv481n106
Supporting Variantsnssv3982784, nssv3988980
SamplesKWS2, KWS1
Known GenesKCNMA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111870
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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